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Anticancer effects of Bilberry anthocyanins compared with NutraNanoSphere encapsulated Bilberry anthocyanins

机译:越橘花青素与NutraNanoSphere封装的越橘花青素的抗癌作用

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摘要

Rapidly accumulating laboratory and clinical research evidence indicates that anthocyanins exhibit anticancer activity and the evaluation of bilberry anthocyanins as chemo-preventive agents is progressing. It has previously been demonstrated that anthocyanins upregulate tumor suppressor genes, induce apoptosis in cancer cells, repair and protect genomic DNA integrity, which is important in reducing age-associated oxidative stress, and improve neuronal and cognitive brain function. Bilberry anthocyanins have pronounced health effects, even though they have a low bioavailability. To increase the bioavailability, Bilberry was encapsulated in 5.5 nm diameter liposomal micelles, called NutraNanoSpheres (NNS), at a concentration of 2.5 mg/50 µl [25% (w/w) anthocyanins]. These Bilberry NNS were used to study the apoptotic/cytotoxic effects on K562 Human Erythroleukemic cancer cells. Flow cytometric fluorescent quantification of the uptake of propidium iodide in a special cell viability formulation into dead K562 cells was used to determine the effects of Bilberry on the viability of K562 cells. The concentrations of Bilberry that demonstrated the greatest levels of percentage inhibition, relative to the control populations, were biphasic, revealing a 60–70% inhibition between 0.018–1.14 mg/ml (n=6) and 60% inhibition at 4 mg/ml. The lowest percentage inhibition (30%) occurred at 2 mg/ml. The lethal dose 50 was determined to be 0.01–0.04 mg/ml of Bilberry per 105 K562 cells at 72 h of cell culture exposure. At 48 h incubation, the highest percentage of inhibition was only 27%, suggesting involvement of a long-term apoptotic event. These levels, which demonstrated direct cytotoxic effects, were 8–40 times lower than levels required for Bilberry that is not encapsulated. The increase in bioavailability with the Bilberry NNS and its water solubility demonstrated the feasibility of using Bilberry NNS in cancer patient clinical trials.
机译:迅速积累的实验室和临床研究证据表明,花色苷具有抗癌活性,而作为化学预防剂的越桔花色苷的评价也在不断发展。以前已经证明,花青素上调肿瘤抑制基因,诱导癌细胞凋亡,修复和保护基因组DNA完整性,这对于减少与年龄相关的氧化应激和改善神经元和认知脑功能很重要。越桔花色苷具有显着的健康作用,即使它们的生物利用度较低。为了提高生物利用度,将越桔以2.5 mg / 50 µl [25%(w / w)花青素]的浓度封装在直径为5.5 nm的脂质体微团中,称为NutraNanoSpheres(NNS)。这些越桔NNS被用于研究对K562人红细胞白血病癌细胞的凋亡/细胞毒性作用。流式细胞术荧光定量分析了特殊细胞活力制剂中碘化丙锭对死亡的K562细胞的摄取,用于确定越桔对K562细胞活力的影响。相对于对照种群,表现出最大百分比抑制水平的越桔浓度是双相的,显示出0.018-1.14 mg / ml(n = 6)的60-70%抑制和4 mg / ml的60%抑制。 。最低的抑制百分比(30%)发生在2 mg / ml。在暴露于细胞培养72小时后,确定的致死剂量50为每105 K562细胞0.01-0.04 mg / ml越桔。孵育48小时后,抑制的最高百分比仅为27%,表明涉及长期的凋亡事件。这些水平显示出直接的细胞毒作用,比未封装的越桔所需水平低8-40倍。 Bilberry NNS的生物利用度及其水溶性的增加证明了在癌症患者临床试验中使用Bilberry NNS的可行性。

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